Name: isolation of active caenorhabditis elegans nuclear extract and reconstitution for in vitro transcription
Uploaded: 2021-08-11T14:00:00.000+00:00
Duration: 6 min 9 s
Description: Watch this Scientific Journal Video about Isolation of Active Caenorhabditis elegans Nuclear Extract and Reconstitution for In Vitro Transcription at JoVE.com

This work was supported by an NIH MIRA grant (R35GM124678 to J. S.).

<ol>
	<li>Corsi, A. K., Wightman, B., Chalfie, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+Transparent+window+into+biology:+A+on+Caenorhabditis+elegans.">A Transparent window into biology: A on Caenorhabditis elegans.</a> Genetics. 200 (2), 387-407 (2015).</li><li>Blackwell, T. K., Walker, A. K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Transcription+mechanisms.">Transcription mechanisms.</a> WormBook: The Online Review of C. elegans Biology. , 1-16 (2006).</li><li>Page, A. P., Johnstone, I. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+cuticle.">The cuticle.</a> WormBook: The Online Review of C. elegans Biology. , 1-15 (2007).</li><li>Lichtsteiner, S., Tjian, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cloning+and+properties+of+the+Caenorhabditis+elegans+TATA-box-binding+protein.">Cloning and properties of the Caenorhabditis elegans TATA-box-binding protein.</a> Proceedings of the National Academy of Sciences of the United States of America. 90 (20), 9673-9677 (1993).</li><li>Lichtsteiner, S., Tjian, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Synergistic+activation+of+transcription+by+UNC-86+and+MEC-3+in+Caenorhabditis+elegans+embryo+extracts.">Synergistic activation of transcription by UNC-86 and MEC-3 in Caenorhabditis elegans embryo extracts.</a> EMBO Journal. 14 (16), 3937-3945 (1995).</li><li>Shan, G., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Isotope-labeled+immunoassays+without+radiation+waste.">Isotope-labeled immunoassays without radiation waste.</a> Proceedings of the National Academy of Sciences of the United States of America. 97 (6), 2445-2449 (2000).</li><li>Voss, C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+novel,+non-radioactive+eukaryotic+in+vitro+transcription+assay+for+sensitive+quantification+of+RNA+polymerase+II+activity.">A novel, non-radioactive eukaryotic in vitro transcription assay for sensitive quantification of RNA polymerase II activity.</a> BMC Molecular Biology. 15, 7 (2014).</li><li>Wibisono, P., Liu, Y., Sun, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+novel+in+vitro+Caenorhabditis+elegans+transcription+system.">A novel in vitro Caenorhabditis elegans transcription system.</a> BMC Molecular and Cell Biology. 21 (1), 87 (2020).</li><li>Stiernagle, T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Maintenance+of+C.+elegans.">Maintenance of C. elegans.</a> WormBook: The Online Review of C. elegans Biology. , 1-11 (2006).</li><li>Zbacnik, T. J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Role+of+buffers+in+protein+formulations.">Role of buffers in protein formulations.</a> Journal of Pharmaceutical Sciences. 106 (3), 713-733 (2017).</li></ol>

The authors have no competing interests to disclose.

C. elegans is an appealing model organism to study the eukaryotic transcription system because of its low-cost maintenance and the ease of genetic manipulation. Here a protocol for consistent isolation of functionally active nuclear extract from L4 C. elegans is described. Although this protocol focused on visualizing transcription activity, the cDNA produced post-transcriptionally can be quantified using RT-qPCR to obtain a more precise measurement of the transcription activity8. This method of isolating nuclear proteins from C. elegans can help expand the study of the eukaryotic transcription machinery. Since C. elegans is not a culture of cells in a dish or a colony of yeast but rather a free-roaming animal, isolating and researching its nuclear extract may give a clearer insight into how the transcriptional machinery may change over time or in various environments. This allows researchers to take advantage of C. elegans low cost and resilience. C. elegans, unlike other model organisms or cell cultures, is much more forgiving when bacterial or yeast contamination appears. A population of C. elegans can be easily cleaned of contamination using established protocols, saving time and effort when contamination does occur9. Overall, using nuclear extract from C. elegans for biochemical assays can be a more affordable and flexible option as compared to purchasing nuclear extract from a vendor or dealing with less forgiving model organisms.
While this protocol is relatively simple, there are still critical steps that require special attention for the successful isolation of the nuclear extract. It is important that during the preparation of the complete hypotonic and hypertonic buffers, the two solutions are clearly labeled and separated. If the buffers are switched at any point during the isolation, this could lead to inactivation of the nuclear proteins or poor fractionation of the cytosolic proteins from the nuclear proteins. Isolated nuclear proteins should also, if necessary, be diluted in hypertonic buffer, not water or any other solution. The high salt concentration helps preserve the activity of the proteins, and a hypotonic solution can kill this activity10.
Another challenge that may arise during the grinding portion of this protocol comes from debris adhering to the surface of the tungsten balls. While it is stated that the balls should be washed and dried after every grinding cycle, the material will attach to the smooth surface of the balls. This material usually appears as rust-colored rings around the circumference of the balls and is thick enough to block the gap between the ball and the wall of the grinding chamber. This blockage is noticeable as it becomes more and more difficult to push the animals through the grinder, which can eventually lead to muscle injury or rupturing of the syringe. If the tungsten balls begin to show discoloration, soak them in hot water for 5 min then clean the surface with a new scouring pad. Avoid using acidic or basic cleaning solutions. After gently polishing, the tungsten balls should return to their original shine, and it will be noticeably easier to grind samples.
This protocol is designed to isolate whole nuclear extract from C. elegans.&#160;It has not been tested for use on other model organisms. Nuclear extract from other organisms may require different buffers, and the CMV promoter may not be enough to drive transcription in other non-mammalian samples. The nuclear extract collected using this method is also not tissue or cell-specific; any transcription activity measured using this method looks at the animals as a whole which may hide the subtle changes between tissues.
Future uses of this protocol could be measuring the DNA repair or replication machinery of C. elegans after DNA damage. The cytosolic fraction collected during the isolation process could be utilized to measure the amount of soluble proteins and quantify the activity of these proteins in a manner similar to measuring transcription.

The small, free-living nematode Caenorhabditis elegans is a simple yet powerful model organism for addressing a wide range of biological questions. Since its introduction in 1963, the nematodes have been invaluable to answering questions in neurobiology, metabolism, aging, development, immunity, and genetics1. Some of the animal&#39;s many characteristics that make it an ideal model organism include short generation time, the effectiveness of RNA interference, transparent body, and the completed maps of both its cellular lineage and nervous system.
While the nematode&#39;s contributions to science are vast, they have been under-utilized to elucidate the eukaryotic transcription system, with most of our understanding about these mechanisms coming from studies using nuclear extract from yeast, fruit fly, and mammalian cell culture2. The biggest hurdle that dissuades researchers from extracting functional nuclear extract is the nematode&#39;s tough outer cuticle. This exoskeleton comprises cross-linked collagens, cuticlins, glycoproteins, and lipids, making C. elegans from larval stage to adulthood resistant to protein extraction via chemical or mechanical forces3. An in vitro transcription system using C. elegans nuclear extract was once developed but not widely adopted due to the system&#39;s limited scope, and the use of Dounce homogenizer for preparing the extract could lead to protein instability4,5.
Unlike the previous protocol for nuclear extract isolation which utilized a Dounce homogenizer to break C. elegans, this protocol uses a Balch homogenizer. The Balch homogenizer consists of two main components: a tungsten carbide ball and a stainless-steel block with a channel bored through from one end to another. The Balch homogenizer is loaded with the tungsten carbide ball and capped on either side to seal the grinding chamber. Syringes can be loaded on the two vertical ports leading into the grinding chamber. As the material is passed from one syringe to the other through the grinding chamber, the pressure from the syringes forces the material through a narrow gap between the ball and the wall of the chamber. This slow and constant pressure breaks the material until it reaches a consistent size that is able to pass through the narrow gap easily. Forcing C. elegans through the narrow gap via a constant yet gentle pressure breaks the animals open, releasing their content into the surrounding buffer. Switching ball sizes further tightens the gap, breaking the newly released cells and frees the nuclei into the buffer. Multiple instances of centrifugation separate the nuclei from the rest of the cell debris, allowing for the collection of a clean nuclear extract. The Balch homogenizer is preferred over the Dounce homogenizer for several reasons: the system can handle a large number of animals, making it possible to extract a high amount of active proteins in a single attempt; the precise machining of the balls and the steel block allows for consistent grinding between multiple samples; the heavy steel block act as a heat sink, uniformly drawing heat away from the grinding chamber, preventing denaturing.
After isolation, the nuclear extract transcriptional activity must be verified before being used in any biochemical experiments. Traditionally, transcription activity was measured using radiolabeled nucleotides to track and visualize the newly synthesized RNA. However, radioactive labeling can be burdensome as it requires precaution during use and disposal6. Technological advancements allow researchers today to use much less harmful or troublesome methods to measure even small RNA quantities using techniques such as quantitative real-time PCR (qRT-PCR)7. Here, the protocol describes a method to isolate active nuclear extract from larval stage 4 (L4) C. elegans and visualize transcription activity in an in vitro system.

<table><tbody><tr><td>&lt;strong&gt;Consumables and reagents&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>0.2 mL 8-Strip Tubes &amp;amp; Flat Strip Caps, Clear</td><td>Genesee Scientific</td><td>&amp;nbsp;24-706</td><td></td></tr><tr><td>0.2 mL Individual PCR tubes</td><td>Genesee Scientific</td><td>&amp;nbsp;24-153G</td><td></td></tr><tr><td>1.7 mL sterile microtubes</td><td>Genesee Scientific</td><td>24-282S</td><td></td></tr><tr><td>100% absolute molecular grade ethanol</td><td>Fisher Scientific</td><td>&amp;nbsp;BP2818</td><td></td></tr><tr><td>100% ethanol, Koptec</td><td>Decon Labs</td><td>&amp;nbsp;V1001</td><td></td></tr><tr><td>10 mL serological pipet</td><td>VWR international</td><td>&amp;nbsp;89130-898</td><td></td></tr><tr><td>150 mm petri plates</td><td>Tritech Research</td><td>&amp;nbsp;T3325</td><td></td></tr><tr><td>15 mL conical centrifuge tubes</td><td>Genesee Scientific</td><td>&amp;nbsp;28-103</td><td></td></tr><tr><td>20 mL plastic syringes</td><td>Fisher Scientific</td><td>14955460</td><td></td></tr><tr><td>2 mL Norm-Ject syringes</td><td>Henke-Sass Wolf GmbH</td><td>4020</td><td></td></tr><tr><td>500 mL vacuum filter cup 0.22 &amp;micro;m PES, Stericup Millipore Express Plus</td><td>Millipore Sigma</td><td>SCGPU10RE</td><td></td></tr><tr><td>50 mL conical centrifuge tubes</td><td>ThermoFisher Scientific</td><td>339652</td><td></td></tr><tr><td>50 mL serological pipet</td><td>VWR international</td><td>&amp;nbsp;89130-902</td><td></td></tr><tr><td>5 mL serological pipet</td><td>VWR international</td><td>&amp;nbsp;89130-896</td><td></td></tr><tr><td>Agar, Criterion</td><td>VWR International</td><td>&amp;nbsp;C7432</td><td></td></tr><tr><td>Agarose</td><td>Denville Scientific</td><td>&amp;nbsp;CA3510-6</td><td></td></tr><tr><td>Alcohol proof marker</td><td>VWR International</td><td>&amp;nbsp;52877-310</td><td></td></tr><tr><td>Bacto peptone</td><td>VWR International</td><td>&amp;nbsp;90000-264</td><td></td></tr><tr><td>&lt;em&gt;Caenorhabditis elegans&lt;/em&gt;</td><td>CGC</td><td>N2</td><td></td></tr><tr><td>Calcium dichloride</td><td>Millipore Sigma</td><td>&amp;nbsp;C4901</td><td></td></tr><tr><td>Cholesterol</td><td>Millipore Sigma</td><td>&amp;nbsp;C8667</td><td></td></tr><tr><td>Control DNA temple cloning primers, Forward 5&amp;rsquo;- ctc atg ttt gac agc tta tcg atc cgg gc -3&amp;rsquo;</td><td></td><td></td><td></td></tr><tr><td>Control DNA temple cloning primers, Forward 5&amp;rsquo;- aca gga cgg gtg tgg tcg cca tga t -3&amp;rsquo;</td><td></td><td></td><td></td></tr><tr><td>Deionized water</td><td></td><td></td><td></td></tr><tr><td>Dithiothreitol</td><td>Invitrogen</td><td>&amp;nbsp;15508-013</td><td></td></tr><tr><td>DNA gel stain, SYBR safe</td><td>Invitrogen</td><td>&amp;nbsp;S33102</td><td></td></tr><tr><td>DNA ladder mix, O&amp;rsquo;gene ruler</td><td>Fisher Scientific</td><td>&amp;nbsp;SM1173</td><td></td></tr><tr><td>DNA Loading Dye, 6x TriTrack</td><td>Fisher Scientific</td><td>&amp;nbsp;FERR1161</td><td></td></tr><tr><td>DNase, Baseline-ZERO</td><td>Lucigen</td><td>&amp;nbsp;DB0715K</td><td></td></tr><tr><td>Dry ice</td><td></td><td></td><td></td></tr><tr><td>&lt;em&gt;Escherichia coli&lt;/em&gt; OP50 strain</td><td>CGC</td><td>OP50</td><td></td></tr><tr><td>Glacial acetic acid</td><td>Fisher Scientific</td><td>&amp;nbsp;A38</td><td></td></tr><tr><td>Glycerol</td><td>Millipore Sigma</td><td>&amp;nbsp;G6279</td><td></td></tr><tr><td>HeLa nuclear extract in vitro transcription system, HeLaScribe</td><td>Promega</td><td>&amp;nbsp;E3110</td><td></td></tr><tr><td>Hepes Solution, 1 M Gibco</td><td>Millipore Sigma</td><td>15630080</td><td></td></tr><tr><td>Hydrochloric acid 37%</td><td>Millipore Sigma</td><td>&amp;nbsp;P0662</td><td></td></tr><tr><td>Hypochlorite bleach</td><td>Clorox</td><td></td><td></td></tr><tr><td>LB Broth</td><td>Millipore Sigma</td><td>&amp;nbsp;L3022</td><td></td></tr><tr><td>Magnesium dichloride</td><td>Millipore Sigma</td><td>&amp;nbsp;M8266</td><td></td></tr><tr><td>Magnesium Sulfate</td><td>Millipore Sigma</td><td>&amp;nbsp;M7506</td><td></td></tr><tr><td>Medium weigh dishes</td><td>Fisher Scientific</td><td>&amp;nbsp;02-202-101</td><td></td></tr><tr><td>microscope slides, Vista vision</td><td>VWR International</td><td>16004-368</td><td></td></tr><tr><td>molecular grade water, Hypure</td><td>Hyclone Laboratories</td><td>&amp;nbsp;SH30538</td><td></td></tr><tr><td>Nystatin</td><td>Millipore Sigma</td><td>&amp;nbsp;N1638</td><td></td></tr><tr><td>PCR system, FailSafe with premix A</td><td>Lucigen</td><td>&amp;nbsp;FS99100</td><td></td></tr><tr><td>Potassium chloride</td><td>Millipore Sigma</td><td>&amp;nbsp;P39111</td><td></td></tr><tr><td>Potassium phosphate dibasic</td><td>Millipore Sigma</td><td>&amp;nbsp;P3786</td><td></td></tr><tr><td>Potassium phosphate monobasic</td><td>Millipore Sigma</td><td>&amp;nbsp;P0662</td><td></td></tr><tr><td>Protease inhibitor, Halt single use cocktail 100x</td><td>ThermoFisher Scientific</td><td>78430</td><td></td></tr><tr><td>protein assay kit, Qubit</td><td>ThermoFisher Scientific</td><td>&amp;nbsp;Q33211</td><td></td></tr><tr><td>reverse transcription kit, Sensiscript</td><td>Qiagen</td><td>205211</td><td></td></tr><tr><td>RNA extraction kit RNeasy micro kit</td><td>Qiagen</td><td>74004</td><td></td></tr><tr><td>RNase Inhibitor</td><td>Applied Biosystems</td><td>&amp;nbsp;N8080119</td><td></td></tr><tr><td>Sodium Chloride</td><td>VWR International</td><td>&amp;nbsp;BDH9286-12KG</td><td></td></tr><tr><td>Sodium hydroxide</td><td>Millipore Sigma</td><td>&amp;nbsp;1-09137</td><td></td></tr><tr><td>Sterile syringe filter with 0.2 &amp;micro;m Polyethersulfone membrane</td><td>VWR international</td><td>28145-501</td><td></td></tr><tr><td>Sucrose</td><td>VWR International</td><td>&amp;nbsp;200-334-9</td><td></td></tr><tr><td>transcription primers, Forward 5&amp;rsquo;- gcc ggg cct ctt gcg gga tat -3&amp;rsquo;</td><td></td><td></td><td></td></tr><tr><td>transcription primers, Reverse 5&amp;rsquo;- cgg cca aag cgg tcg gac agt-3&amp;rsquo;</td><td></td><td></td><td></td></tr><tr><td>Tris-Base</td><td>Fisher Scientific</td><td>&amp;nbsp;BP152</td><td></td></tr><tr><td>Tween20</td><td>Millipore Sigma</td><td>&amp;nbsp;P2287</td><td></td></tr><tr><td>&lt;strong&gt;Equipment&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>-20 &amp;deg;C incubator</td><td>ThermoFisher Scientific</td><td></td><td></td></tr><tr><td>20 &amp;deg;C incubator</td><td>ThermoFisher Scientific</td><td></td><td></td></tr><tr><td>37 &amp;deg;C incubator</td><td>Forma Scientific</td><td></td><td></td></tr><tr><td>4 &amp;deg;C refrigerator</td><td>ThermoFisher Scientific</td><td></td><td></td></tr><tr><td>-80 &amp;deg;C freezer</td><td>Eppendorf</td><td></td><td></td></tr><tr><td>Autoclave</td><td>Sanyo</td><td></td><td></td></tr><tr><td>Balch homogenizer, isobiotec cell homogenizer</td><td>Isobiotec</td><td></td><td></td></tr><tr><td>Benchtop Vortexer</td><td>Fisher Scientific</td><td>2215365</td><td></td></tr><tr><td>Centrifuge, Eppendorf 5418 R</td><td>Eppendorf</td><td>5401000013</td><td></td></tr><tr><td>Centrifuge, VWR Clinical 50</td><td>VWR International</td><td>82013-800</td><td></td></tr><tr><td>Dissection microscope, Leica M80</td><td>Leica Microsystems</td><td></td><td></td></tr><tr><td>Fluorometer, Qubit 2.0</td><td>Invitrogen</td><td>Q32866</td><td></td></tr><tr><td>Gel imaging system, iBright FL1500</td><td>ThermoFisher Scientific</td><td>&amp;nbsp;A44241</td><td></td></tr><tr><td>Gel system</td><td>ThermoFisher Scientific</td><td></td><td></td></tr><tr><td>Heat block</td><td>VWR International</td><td>12621-048</td><td></td></tr><tr><td>Microcentrifuges, Eppendorf 5424</td><td>Eppendorf</td><td>22620401</td><td></td></tr><tr><td>PIPETBOY acu 2</td><td>Integra</td><td>155017</td><td></td></tr><tr><td>Pipette L-1000 XLS+, Pipet-Lite LTS</td><td>Rainin</td><td>17014382</td><td></td></tr><tr><td>Pipette L-10 XLS+, Pipet-Lite LTS</td><td>Rainin</td><td>17014388</td><td></td></tr><tr><td>Pipette L-200 XLS+, Pipet-Lite LTS</td><td>Rainin</td><td>17014391</td><td></td></tr><tr><td>Pipette L-20 XLS+, Pipet-Lite LTS</td><td>Rainin</td><td>17014392</td><td></td></tr><tr><td>Rocking platform</td><td>VWR International</td><td></td><td></td></tr><tr><td>Thermocycler, Eppendorf Mastercycler Pro</td><td>Eppendorf</td><td>950030010</td><td></td></tr></tbody></table>

isolation of active caenorhabditis elegans nuclear extract and reconstitution for in vitro transcription

Caenorhabditis elegans has been an important model system for biological research since it was introduced in 1963. However, C. elegans has not been fully utilized in the biochemical study of biological reactions using its nuclear extracts such as in vitro transcription and DNA replication. A significant hurdle for using C. elegans in biochemical studies is disrupting the nematode&#39;s thick outer cuticle without sacrificing the activity of the nuclear extract. While several methods are used to break the cuticle, such as Dounce homogenization or sonication, they often lead to protein instability. There are no established protocols for isolating active nuclear proteins from larva or adult C. elegans for in vitro reactions. Here, the protocol describes in detail the homogenization of larval stage 4 C. elegans using a Balch homogenizer. The Balch homogenizer uses pressure to slowly force the animals through a narrow gap breaking the cuticle in the process. The uniform design and precise machining of the Balch homogenizer allow for consistent grinding of animals between experiments. Fractionating the homogenate obtained from the Balch homogenizer yields functionally active nuclear extract that can be used in an in vitro method for assaying transcription activity of C. elegans.

Following the outlined steps should yield functional nuclear extract (Figure 1), deviation in the grinding or wash steps can lead to poor activity or low yields. If functional C. elegans nuclear extract is obtained, it will transcribe the region downstream of the CMV promoter on the DNA template when added to the previously described in vitro assay. The resulting RNA transcript can be purified from the nuclear proteins and DNA template using conventional methods. Without the template DNA, reverse transcription and subsequent PCR product can only be the result of the RNA transcribed by the nuclear extract. The PCR products can be visualized on an agarose gel, the intensity of the DNA band can be indicative of the quality of nuclear protein and RNA isolation. A weak band intensity can be caused by the inactivation of the nuclear extract either by heat or poor buffer preparation. An excessively strong band intensity can be the result of DNA contamination either due to poor RNA purification or improper DNase digestion. Consistent and successful nuclear isolations will produce bands of similar intensities, and both transcriptional and PCR negative controls should have no visible PCR product (Figure 2).
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/62723/62723fig1v2.jpg" /> 
Figure 1. An outline of nuclear extract isolation. The flowchart outlines the major steps for isolating nuclear extract from C. elegans. <a href="https://www.jove.com/files/ftp_upload/62723/62723fig1v2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/62723/62723fig02.jpg" /> 
Figure 2. C. elegans nuclear extract retains its activity. The gel image shows the transcription products of C. elegans L4 larvae nuclear extract using the CMV promoter DNA template. Successful isolation of active nuclear proteins will result in a 132 bp PCR product after in vitro transcription, as seen in lanes 1 and 2. Unsuccessful isolation will result in a weak band or the absence of a PCR product similar to lane 3. This visualization of the transcription activity via PCR amplification is a simple way to assess the quality of the nuclear extraction isolation. The positive PCR control is produced by adding the CMV promoter DNA template to the PCR reaction, and the negative control is lacking the template DNA. <a href="https://www.jove.com/files/ftp_upload/62723/62723fig02large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Nematode Growth Media Plates</td>
			<td></td>
		</tr>
		<tr>
			<td>Agar</td>
			<td>20.4 g</td>
		</tr>
		<tr>
			<td>Sodium Chloride</td>
			<td>2.8 g</td>
		</tr>
		<tr>
			<td>Bacto peptone</td>
			<td>2.3 g</td>
		</tr>
		<tr>
			<td>dH2O</td>
			<td>975 mL</td>
		</tr>
		<tr>
			<td colspan="2">Autoclave at 121 &#176;C for 30 min</td>
		</tr>
		<tr>
			<td colspan="2">Allow the media to cool to 50 &#176;C before adding the following</td>
		</tr>
		<tr>
			<td>1 M CaCl2 (Sterile)</td>
			<td>1 mL</td>
		</tr>
		<tr>
			<td>1 M MgSO4 (Sterile)</td>
			<td>1 mL</td>
		</tr>
		<tr>
			<td>10,000 units/mL Nystatin (Sterile)</td>
			<td>3 mL</td>
		</tr>
		<tr>
			<td>5 mg/mL Cholesterol in 95% Ethanol (Filter Sterilized)</td>
			<td>1 mL</td>
		</tr>
		<tr>
			<td>1M KPO4&#160;pH 6.0 (Sterile)</td>
			<td>25 mL</td>
		</tr>
	</tbody>
</table>
Table 1.
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>M9 Buffer</td>
			<td></td>
		</tr>
		<tr>
			<td>KH2PO4</td>
			<td>3 g</td>
		</tr>
		<tr>
			<td>Na2HPO4</td>
			<td>6 g</td>
		</tr>
		<tr>
			<td>NaCl</td>
			<td>5 g</td>
		</tr>
		<tr>
			<td>dH2O</td>
			<td>1,000 mL</td>
		</tr>
		<tr>
			<td colspan="2">Autoclave at 121 &#176;C for 15 min</td>
		</tr>
		<tr>
			<td>1 M MgSO4 (Sterile)</td>
			<td>1 mL (add after autoclaving)</td>
		</tr>
		<tr>
			<td>S-basal Buffer</td>
			<td></td>
		</tr>
		<tr>
			<td>KH2PO4</td>
			<td>6 g</td>
		</tr>
		<tr>
			<td>K2HPO4</td>
			<td>1 g</td>
		</tr>
		<tr>
			<td>NaCl</td>
			<td>5.85 g</td>
		</tr>
		<tr>
			<td>dH2O</td>
			<td>1,000 mL</td>
		</tr>
		<tr>
			<td colspan="2">Autoclave at 121 &#176;C for 15 min</td>
		</tr>
		<tr>
			<td>Cholesterol 5 mg/mL (Sterile)</td>
			<td>1 mL (add after autoclaving)</td>
		</tr>
	</tbody>
</table>
Table 2.
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td colspan="3">Hypotonic Buffer</td>
		</tr>
		<tr>
			<td>Stock Solution</td>
			<td>Volume</td>
			<td>Final concentration</td>
		</tr>
		<tr>
			<td>1 M HEPES KOH pH 7.6</td>
			<td>7.5 mL</td>
			<td>15 mM</td>
		</tr>
		<tr>
			<td>1 M KCl</td>
			<td>5.0 mL</td>
			<td>10 mM</td>
		</tr>
		<tr>
			<td>1 M MgCl2</td>
			<td>2.5 mL</td>
			<td>5 mM</td>
		</tr>
		<tr>
			<td>0.5 M EDTA</td>
			<td>0.1 mL</td>
			<td>0.1 mM</td>
		</tr>
		<tr>
			<td>1 M Sucrose</td>
			<td>175 mL</td>
			<td>350 mM</td>
		</tr>
		<tr>
			<td>dH2O</td>
			<td>309.9 mL</td>
			<td></td>
		</tr>
		<tr>
			<td colspan="3">Filter sterilize</td>
		</tr>
	</tbody>
</table>
Table 3.
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td colspan="3">Hypertonic Buffer</td>
		</tr>
		<tr>
			<td>Stock Solution</td>
			<td>Volume</td>
			<td>Final Concentration</td>
		</tr>
		<tr>
			<td>1 M HEPES KOH pH 7.6</td>
			<td>7.5 mL</td>
			<td>15 mM</td>
		</tr>
		<tr>
			<td>1 M KCl</td>
			<td>200 mL</td>
			<td>400 mM</td>
		</tr>
		<tr>
			<td>1 M MgCl2</td>
			<td>2.5 mL</td>
			<td>5 mM</td>
		</tr>
		<tr>
			<td>0.5 M EDTA</td>
			<td>0.1 mL</td>
			<td>0.1 mM</td>
		</tr>
		<tr>
			<td>10% Tween 20</td>
			<td>5 mL</td>
			<td>0.10%</td>
		</tr>
		<tr>
			<td>50% Glycerol</td>
			<td>100 mL</td>
			<td>10%</td>
		</tr>
		<tr>
			<td>dH2O</td>
			<td>184.9 mL</td>
			<td></td>
		</tr>
		<tr>
			<td colspan="3">Filter sterilize</td>
		</tr>
	</tbody>
</table>
Table 4.
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>MgCl2, 50 mM</td>
			<td>1.5 &#181;L</td>
		</tr>
		<tr>
			<td>rNTP mix, 10 mM each</td>
			<td>1.0 &#181;L</td>
		</tr>
		<tr>
			<td>Template DNA, 25 ng/&#181;L</td>
			<td>4.0 &#181;L</td>
		</tr>
		<tr>
			<td>RNase-free H2O</td>
			<td>7.5 &#181;L</td>
		</tr>
	</tbody>
</table>
Table 5.
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Step</td>
			<td>Temp</td>
			<td>Time</td>
			<td>Cycle number</td>
		</tr>
		<tr>
			<td>Preheat</td>
			<td>37 &#176;C</td>
			<td>60 min</td>
			<td>1x</td>
		</tr>
		<tr>
			<td>Reverse Transcription</td>
			<td>37 &#176;C</td>
			<td>60 min</td>
			<td>1x</td>
		</tr>
		<tr>
			<td>Hold</td>
			<td>10 &#176;C</td>
			<td></td>
			<td>1x</td>
		</tr>
	</tbody>
</table>
Table 6.
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>10x Reverse Transcription Buffer</td>
			<td>2.0 &#181;L</td>
		</tr>
		<tr>
			<td>dNTP Mix (5 mM each dNTP)</td>
			<td>2.0 &#181;L</td>
		</tr>
		<tr>
			<td>Transcription Reverse Primer (10 &#181;M)</td>
			<td>2.0 &#181;L</td>
		</tr>
		<tr>
			<td>RNase Inhibitor</td>
			<td>1.0 &#181;L</td>
		</tr>
		<tr>
			<td>Sensiscript Reverse Transcriptase</td>
			<td>1.0 &#181;L</td>
		</tr>
		<tr>
			<td>RNase-free H2O</td>
			<td>10.0 &#181;L</td>
		</tr>
	</tbody>
</table>
Table 7.
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>RNase-Free H2O</td>
			<td>6.25 &#181;L</td>
		</tr>
		<tr>
			<td>Transcription Forward Primer (10 &#181;M)</td>
			<td>2.5 &#181;L</td>
		</tr>
		<tr>
			<td>Transcription Reverse Primer (10 &#181;M)</td>
			<td>2.5 &#181;L</td>
		</tr>
		<tr>
			<td>PCR 2X Premix A</td>
			<td>12.5 &#181;L</td>
		</tr>
		<tr>
			<td>PCR Enzyme Mix</td>
			<td>0.25 &#181;L</td>
		</tr>
	</tbody>
</table>
Table 8.
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Step</td>
			<td>Temp</td>
			<td>Time</td>
			<td>Cycle number</td>
		</tr>
		<tr>
			<td>Initial Denature</td>
			<td>92 &#176;C</td>
			<td>60 s</td>
			<td>1x</td>
		</tr>
		<tr>
			<td>Denature</td>
			<td>92 &#176;C</td>
			<td>30 s</td>
			<td></td>
		</tr>
		<tr>
			<td>Anneal</td>
			<td>59 &#176;C</td>
			<td>30 s</td>
			<td>35x</td>
		</tr>
		<tr>
			<td>Extension</td>
			<td>72 &#176;C</td>
			<td>30 s</td>
			<td></td>
		</tr>
		<tr>
			<td>Hold</td>
			<td>10 &#176;C</td>
			<td></td>
			<td>1x</td>
		</tr>
	</tbody>
</table>
Table 9.

Watch this Scientific Journal Video about Isolation of Active Caenorhabditis elegans Nuclear Extract and Reconstitution for In Vitro Transcription at JoVE.com

Isolation of Active Caenorhabditis elegans Nuclear Extract and Reconstitution for In Vitro Transcription

Here, we describe a detailed protocol for isolating active nuclear extract from larval stage 4 C. elegans and visualizing transcription activity in an in vitro system.

Isolation of Active Caenorhabditis elegans Nuclear Extract and Reconstitution for In Vitro Transcription

Caenorhabditis elegans has been an important model system for biological research since it was introduced in 1963. However, C. elegans has not been fully ...

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Nanyang Technological University

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Biochemistry

2.5K Views.  Washington State University. Here, we describe a detailed protocol for isolating active nuclear extract from larval stage 4 C. elegans and visualizing transcription activity in an in vitro system.

Video: Isolation of Active Caenorhabditis elegans Nuclear Extract and Reconstitution for In Vitro Transcription

An Oligonucleotide-based Tandem RNA Isolation Procedure to Recover Eukaryotic mRNA-Protein Complexes

RNA-binding proteins (RBPs) play key roles in the post-transcriptional control of gene expression. Therefore, biochemical characterization of mRNA-protein complexes is essential to understanding mRNA regulation inferred by interacting proteins or non-coding RNAs. Herein, we describe a tandem RNA isolation procedure (TRIP) that enables the purification of endogenously formed mRNA-protein complexes from cellular extracts. The two-step protocol involves the isolation of polyadenylated mRNAs with antisense oligo(dT) beads and subsequent capture of an mRNA of interest with 3&#39;-biotinylated 2&#39;-O-methylated antisense RNA oligonucleotides, which can then be isolated with streptavidin beads. TRIP was used to recover in vivo crosslinked mRNA-ribonucleoprotein (mRNP) complexes from yeast, nematodes and human cells for further RNA and protein analysis. Thus, TRIP is a versatile approach that can be adapted to all types of polyadenylated RNAs across organisms to study the dynamic re-arrangement of mRNPs imposed by intracellular or environmental cues.

A tandem RNA isolation procedure (TRIP) for recovery of endogenously formed mRNA-protein complexes is described. Specifically, RNA-protein complexes are crosslinked in vivo, polyadenylated RNAs are isolated from extracts with oligo(dT) beads, and particular mRNAs are captured with modified RNA antisense oligonucleotides. Proteins bound to mRNAs are detected by immunoblot analysis.

RNA-binding proteins (RBPs) play key roles in the post-transcriptional control of gene expression. Therefore, biochemical characterization of mRNA-protein ...

Application of RNAi and Heat-shock-induced Transcription Factor Expression to Reprogram Germ Cells to Neurons in C. elegans

Studying the cell biological processes during converting the identities of specific cell types provides important insights into mechanism that maintain and protect cellular identities. The conversion of germ cells into specific neurons in the nematode Caenorhabditis elegans (C. elegans) is a powerful tool for performing genetic screens in order to dissect regulatory pathways that safeguard established cell identities. Reprogramming of germ cells to a specific type of neurons termed ASE requires transgenic animals that allow broad over-expression of the Zn-finger transcription factor (TF) CHE-1. Endogenous CHE-1 is expressed exclusively in two head neurons and is required to specify the glutamatergic ASE neurons fate, which can easily be visualized by the gcy-5prom::gfp reporter. A trans gene containing the heat-shock promoter-driven che-1 gene expression construct allows broad mis-expression of CHE-1 in the entire animal upon heat-shock treatment. The combination of RNAi against the chromatin-regulating factor LIN-53 and heat-shock-induced che-1 over-expression leads to reprogramming of germ cell into ASE neuron-like cells. We describe here the specific RNAi procedure and appropriate conditions for heat-shock treatment of transgenic animals in order to successfully induce germ cell to neuron conversion.

Application of RNAi and Heat-shock-induced Transcription Factor Expression to Reprogram Germ Cells to Neurons in C. elegans

This protocol describes how to study cellular processes during cell fate conversion in Caenorhabditis elegans in vivo. Using transgenic animals, allowing heat-shock promoter-driven overexpression of the neuron fate-inducing transcription factor CHE-1 and RNAi-mediated depletion of the chromatin-regulating factor LIN-53 germ cell to neuron reprogramming can be observed in vivo.

Studying the cell biological processes during converting the identities of specific cell types provides important insights into mechanism that maintain ...

Developmental Biology

Isolation of Specific Neuron Populations from Roundworm Caenorhabditis elegans

During the aging process, many cells accumulate high levels of damage leading to cellular dysfunction, which underlies many geriatric and pathological conditions. Post-mitotic neurons represent a major cell type affected by aging. Although multiple mammalian models of neuronal aging exist, they are challenging and expensive to establish. The roundworm Caenorhabditis elegans is a powerful model to study neuronal aging, as these animals have short lifespan, an available robust genetic toolbox, and well-cataloged nervous system. The method presented herein allows for seamless isolation of specific cells based on the expression of a transgenic green fluorescent protein (GFP). Transgenic animal lines expressing GFP under distinct, cell type-specific promoters are digested to remove the outer cuticle and gently mechanically disrupted to produce slurry containing various cell types. The cells of interest are then separated from non-target cells through fluorescence-activated cell sorting, or by anti-GFP-coupled magnetic beads. The isolated cells can then be cultured for a limited time or immediately used for cell-specific ex vivo analyses such as transcriptional analysis by real time quantitative PCR. Thus, this protocol allows for rapid and robust analysis of cell-specific responses within different neuronal populations in C. elegans.

Isolation of Specific Neuron Populations from Roundworm Caenorhabditis elegans

Here, we present a protocol for simple isolation of specific groups of live neuronal cells expressing green fluorescent protein from transgenic Caenorhabditis elegans lines. This method enables a variety of ex vivo studies focused on specific neurons and has the capacity to isolate cells for further short-term culturing.

During the aging process, many cells accumulate high levels of damage leading to cellular dysfunction, which underlies many geriatric and pathological ...

Protein Extract Preparation and Co-immunoprecipitation from Caenorhabditis elegans

Co-immunoprecipitation methods are frequently used to study protein-protein interactions. Confirmation of hypothesized protein-protein interactions or identification of new ones can provide invaluable information about the function of a protein of interest. Some of the traditional methods for extract preparation frequently require labor-intensive and time-consuming techniques. Here, a modified extract preparation protocol using a bead mill homogenizer and metal beads is described as a rapid alternative to traditional protein preparation methods. This extract preparation method is compatible with downstream co-immunoprecipitation studies. As an example, the method was used to successfully co-immunoprecipitate&#160;C. elegans microRNA Argonaute ALG-1 and two known ALG-1 interactors: AIN-1, and HRPK-1. This protocol includes descriptions of animal sample collection, extract preparation, extract clarification, and protein immunoprecipitation. The described protocol can be adapted to test for interactions between any two or more endogenous, endogenously tagged, or overexpressed C. elegans proteins in a variety of genetic backgrounds.

Protein Extract Preparation and Co-immunoprecipitation from Caenorhabditis elegans

This method describes a protocol for high-throughput protein extract preparation from Caenorhabditis elegans samples and subsequent co-immunoprecipitation.

Co-immunoprecipitation methods are frequently used to study protein-protein interactions. Confirmation of hypothesized protein-protein interactions or ...

Isolation and In vitro Activation of Caenorhabditis elegans Sperm

Males and hermaphrodites are the two naturally found sexual forms in the nematode C. elegans. The amoeboid sperm are produced by both males and hermaphrodites. In the earlier phase of gametogenesis, the germ cells of hermaphrodites differentiate into limited number of sperm - around 300 - and are stored in a small 'bag' called the spermatheca. Later on, hermaphrodites continually produce oocytes1. In contrast, males produce exclusively sperm throughout their adulthood. The males produce so much sperm that it accounts for &gt;50% of the total cells in a typical adult worm2. Therefore, isolating sperm from males is easier than from that of hermaphrodites.
Only a small proportion of males are naturally generated due to spontaneous non-disjunction of X chromosome3. Crossing hermaphrodites with males or more conveniently, the introduction of mutations to give rise to Him (High Incidence of Males) phenotype are some of strategies through which one can enrich the male population3.
Males can be easily distinguished from hermaphrodites by observing the tail morphology4. Hermaphrodite's tail is pointed, whereas male tail is rounded with mating structures.
Cutting the tail releases vast number of spermatids stored inside the male reproductive tract. Dissection is performed under a stereo microscope using 27 gauge needles. Since spermatids are not physically connected with any other cells, hydraulic pressure expels internal contents of male body, including spermatids2.
Males are directly dissected on a small drop of 'Sperm Medium'. Spermatids are sensitive to alteration in the pH. Hence, HEPES, a compound with good buffering capacity is used in sperm media. Glucose and other salts present in sperm media help maintain osmotic pressure to maintain the integrity of sperm.
Post-meiotic differentiation of spermatids into spermatozoa is termed spermiogenesis or sperm activation. Shakes5, and Nelson6 previously showed that round spermatids can be induced to differentiate into spermatozoa by adding various activating compounds including Pronase E. Here we demonstrate in vitro spermiogenesis of C. elegans spermatids using Pronase E.
Successful spermiogenesis is pre-requisite for fertility and hence the mutants defective in spermiogenesis are sterile. Hitherto several mutants have been shown to be defective specifically in spermiogenesis process7. Abnormality found during in vitro activation of novel Spe (Spermatogenesis defective) mutants would help us discover additional players participating in this event.

Isolation and In vitro Activation of Caenorhabditis elegans Sperm

A protocol for isolating and activating spermatids from male C. elegans is described here. Cutting the posterior end of male releases spermatids. The spermatids can be activated by addition of protease.

Males and hermaphrodites are the two naturally found sexual forms in the nematode C. elegans. The amoeboid sperm are produced by both males and ...

Biology

Small-scale Nuclear Extracts for Functional Assays of Gene-expression Machineries

A great deal of progress in understanding gene expression has been made using in vitro systems. For most studies, functional assays are carried out using extracts that are prepared in bulk from 10-50 or more liters of cells grown in suspension. However, these large-scale preparations are not amenable to rapidly testing in vitro effects that result from a variety of in vivo cellular treatments or conditions. This journal video article shows a method for preparing functional small-scale nuclear extracts, using HeLa cells as an example. This method is carried out using as few as three 150 mm plates of cells grown as adherent monolayers. To illustrate the efficiency of the small-scale extracts, we show that they are as active as bulk nuclear extracts for coupled RNA Polymerase II transcription/splicing reactions. To demonstrate the utility of the extract protocol, we show that splicing is abolished in extracts prepared from HeLa cells treated with the splicing inhibitor drug E7107. The small-scale protocol should be generally applicable to any process or cell type that can be investigated in vitro using cellular extracts. These include patient cells that are only available in limited quantities or cells exposed to numerous agents such as drugs, DNA damaging agents, RNAi, or transfection, which require the use of small cell populations. In addition, small amounts of freshly grown cells are convenient and/or required for some applications.

A protocol for preparation of robust, small-scale HeLa nuclear extracts is described. This protocol is valuable for assays that require use of small populations of cells, such as cells treated with drugs or RNAi. The method should be applicable to a wide variety of gene expression assays and other cell types, including patient cells.

A great deal of progress in understanding gene expression has been made using in vitro systems.  For most studies, functional assays are carried out using ...

Combined Nucleotide and Protein Extractions in Caenorhabditis elegans

A single biological sample holds a plethora of information, and it is now common practice to simultaneously investigate several macromolecules to capture a full picture of the multiple levels of molecular processing and changes between different conditions. This protocol presents the method of isolating DNA, RNA, and protein from the same sample of the nematode Caenorhabditis elegans to remove the variation introduced when these biomolecules are isolated from replicates of similarly treated but ultimately different samples. Nucleic acids and protein are extracted from the nematode using the acid guanidinium thiocyanate-phenol-chloroform extraction method, with subsequent precipitation, washing, and solubilization of each. We show the successful isolation of RNA, DNA, and protein from a single sample from three strains of nematode and HeLa cells, with better protein isolation results in adult animals. Additionally, guanidinium thiocyanate-phenol-chloroform-extracted protein from nematodes improves the resolution of larger proteins, with enhanced detectable levels as observed by immunoblotting, compared to the traditional RIPA extraction of protein.
The method presented here is useful when investigating samples using a multiomic approach, specifically for the exploration of the proteome and transcriptome. Techniques that simultaneously assess multiomics are appealing because molecular signaling underlying complex biological phenomena is thought to occur at complementary levels; however, it has become increasingly common to see that changes in mRNA levels do not always reflect the same change in protein levels and that the time of collection is relevant in the context of circadian regulations. This method removes any intersample variation when assaying different contents within the same sample (intrasample.)

Combined Nucleotide and Protein Extractions in Caenorhabditis elegans

Here, we present a protocol for the isolation of RNA, DNA, and protein from the same sample, in an effort to reduce variation, improve reproducibility, and facilitate interpretations.

A single biological sample holds a plethora of information, and it is now common practice to simultaneously investigate several macromolecules to capture ...

Small-Scale Extraction of Caenorhabditis elegans Genomic DNA

Genomic DNA extraction from single or a few Caenorhabditis elegans has many downstream applications, including PCR for genotyping lines, cloning, and sequencing. The traditional proteinase K-based methods for genomic DNA extraction from C. elegans take several hours. Commercial extraction kits that effectively break open the C. elegans cuticle and extract genomic DNA are limited. An easy, faster (~15 min), and cost-efficient method of extracting C. elegans genomic DNA that works well for classroom and research applications is reported here. This DNA extraction method is optimized to use single or a few late-larval (L4) or adult nematodes as starting material for obtaining a reliable template to perform PCR. The results indicate that the DNA quality is suitable for amplifying gene targets of different sizes by PCR, permitting genotyping of single or a few animals even at dilutions to one-fiftieth of the genomic DNA from a single adult per reaction. The reported protocols can be reliably used to quickly produce DNA template from a single or a small sample of C. elegans for PCR-based applications.

Small-Scale Extraction of Caenorhabditis elegans Genomic DNA

Presented here is a description of the straightforward and relatively rapid isolation of Caenorhabditis elegans genomic DNA from one or a few animals using a commercially available tissue kit. The resulting gDNA preparation is a suitable template for PCR.

Genomic DNA extraction from single or a few Caenorhabditis elegans has many downstream applications, including PCR for genotyping lines, cloning, and ...

Hand Dissection of Caenorhabditis elegans Intestines

Comprised of only 20 cells, the Caenorhabditis elegans intestine&#160;is the nexus of many life-supporting functions, including digestion, metabolism, aging, immunity, and environmental response. Critical interactions between the C. elegans host and its environment converge within the intestine, where gut microbiota concentrate. Therefore, the ability to isolate intestine tissue away from the rest of the worm is necessary to assess intestine-specific processes. This protocol describes a method for hand dissecting adult C. elegans intestines. The procedure can be performed in fluorescently labeled strains for ease or training purposes. Once the technique is perfected, intestines can be collected from unlabeled worms of any genotype. This microdissection approach allows for the simultaneous capture of host intestinal tissue and gut microbiota, a benefit to many microbiome studies. As such, downstream applications for the intestinal preparations generated by this protocol can include but are not limited to RNA isolation from intestinal cells and DNA isolation from captured microbiota. Overall, hand dissection of C. elegans intestines affords a simple and robust method to investigate critical aspects of intestine biology.

Hand Dissection of Caenorhabditis elegans Intestines

The present protocol describes a procedure for isolating intestines from adult Caenorhabditis elegans nematode worms by hand for input in genomics, proteomics, microbiome, or other assays.

Comprised of only 20 cells, the Caenorhabditis elegans intestine&#160;is the nexus of many life-supporting functions, including digestion, metabolism, ...

Lipid Supplementation for Longevity and Gene Transcriptional Analysis in Caenorhabditis elegans

Aging is a complex process characterized by progressive physiological changes resulting from both environmental and genetic contributions. Lipids are crucial in constituting structural components of cell membranes, storing energy, and as signaling molecules. Regulation of lipid metabolism and signaling is essential to activate distinct longevity pathways. The roundworm Caenorhabditis elegans is an excellent and powerful organism to dissect the contribution of lipid metabolism and signaling in longevity regulation. Multiple research studies have described how diet supplementation of specific lipid molecules can extend C. elegans lifespan; however, minor differences in the supplementation conditions can cause reproducibility issues among scientists in different labs. Here, two detailed supplementation methods for C. elegans are reported employing lipid supplementation either with bacteria seeded on plates or bacterial suspension in liquid culture. Also provided herein are the details to perform lifespan assays with lifelong lipid supplementation and qRT-PCR analysis using a whole worm lysate or dissected tissues derived from a few worms. Using a combination of longitudinal studies and transcriptional investigations upon lipid supplementation, the feeding assays provide dependable approaches to dissect how lipids influence longevity and healthy aging. This methodology can also be adapted for various nutritional screening approaches to assess changes in a subset of transcripts using either a small number of dissected tissues or a few animals.

Lipid Supplementation for Longevity and Gene Transcriptional Analysis in Caenorhabditis elegans

The present protocol describes lipid supplementation methods in liquid and on-plate cultures for Caenorhabditis elegans, coupled with longitudinal studies and gene transcriptional analysis from bulk or a few worms and worm tissues.

Aging is a complex process characterized by progressive physiological changes resulting from both environmental and genetic contributions. Lipids are ...

Isolation of Active Caenorhabditis elegans Nuclear Extract and Reconstitution for In Vitro Transcription

Summary

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Chapters in this video

An Oligonucleotide-based Tandem RNA Isolation Procedure to Recover Eukaryotic mRNA-Protein Complexes

Application of RNAi and Heat-shock-induced Transcription Factor Expression to Reprogram Germ Cells to Neurons in C. elegans

Isolation of Specific Neuron Populations from Roundworm Caenorhabditis elegans

Protein Extract Preparation and Co-immunoprecipitation from Caenorhabditis elegans

Isolation and In vitro Activation of Caenorhabditis elegans Sperm

Small-scale Nuclear Extracts for Functional Assays of Gene-expression Machineries

Combined Nucleotide and Protein Extractions in Caenorhabditis elegans

Small-Scale Extraction of Caenorhabditis elegans Genomic DNA

Hand Dissection of Caenorhabditis elegans Intestines

Lipid Supplementation for Longevity and Gene Transcriptional Analysis in Caenorhabditis elegans